Elucidate the structure for compound Busing spectroscopic data provided. B. Spectral analysis of a pure compound gave the following MS, IR data and H-NMR data (after D2O shake). i) Provide the Molecular formula, (ii) Identify the correct structure (iii) Identify the most important (diagnostic) IR signal(s) and match each proton NMR absorption with the proton that is causing that absorbance? MS: m/z: 86 (10%) ; 87 (0.5); 68.07 (100.0%), 69.08 (5.4%) 1H NMR (d): 5.67 (1H, doublet, J = 18), 5.63 (1H, quartet, J= 17), 4.38 (1H, quartet), 1.63 (3H, doublet), 1.07 (3H, doublet). IR (see below) LOD 4000 3000 2000 HAVENUMBERI-1 1500 1000 500

Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter12: Structure Determination: Mass Spectrometry And Infrared Spectroscopy
Section12.SE: Something Extra
Problem 48AP: The infrared spectrum of the compound with the mass spectrum shown below lacks any significant...
icon
Related questions
Question
2
Elucidate the structure for compound Busing spectroscopic data provided.
B. Spectral analysis of a pure compound gave the following MS, IR data and H-NMR data (after D2O shake). i) Provide the Molecular formula, (ii) Identify the correct structure (iii) Identify
the most important (diagnostic) IR signal(s) and match each proton NMR absorption with the proton that is causing that absorbance?
MS: m/z: 86 (10%) ; 87 (0.5); 68.07 (100.0%), 69.08 (5.4%)
1H NMR (d): 5.67 (1H, doublet, J = 18), 5.63 (1H, quartet, J= 17), 4.38 (1H, quartet), 1.63 (3H, doublet), 1.07 (3H, doublet).
IR (see below)
LOD
4000
3000
2000
HAVENUMBERI
1500
1000
500
Transcribed Image Text:Elucidate the structure for compound Busing spectroscopic data provided. B. Spectral analysis of a pure compound gave the following MS, IR data and H-NMR data (after D2O shake). i) Provide the Molecular formula, (ii) Identify the correct structure (iii) Identify the most important (diagnostic) IR signal(s) and match each proton NMR absorption with the proton that is causing that absorbance? MS: m/z: 86 (10%) ; 87 (0.5); 68.07 (100.0%), 69.08 (5.4%) 1H NMR (d): 5.67 (1H, doublet, J = 18), 5.63 (1H, quartet, J= 17), 4.38 (1H, quartet), 1.63 (3H, doublet), 1.07 (3H, doublet). IR (see below) LOD 4000 3000 2000 HAVENUMBERI 1500 1000 500
Expert Solution
trending now

Trending now

This is a popular solution!

steps

Step by step

Solved in 3 steps with 3 images

Blurred answer
Knowledge Booster
NMR Spectroscopy of Organic Molecules
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.
Similar questions
  • SEE MORE QUESTIONS
Recommended textbooks for you
Organic Chemistry
Organic Chemistry
Chemistry
ISBN:
9781305080485
Author:
John E. McMurry
Publisher:
Cengage Learning
Macroscale and Microscale Organic Experiments
Macroscale and Microscale Organic Experiments
Chemistry
ISBN:
9781305577190
Author:
Kenneth L. Williamson, Katherine M. Masters
Publisher:
Brooks Cole